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Stefania Corti

Showing results (251-260 of 287) with videos related to

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Cell Death Discovery|March 28, 2026
Lithium ameliorates neural differentiation restoring cell death balance in Cornelia de Lange syndrome 2D and 3D modelsChiara Parodi, Antonella Lettieri, Paolo Grazioli, et al.
JAMA Neurology|April 7, 2015
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular AtrophyMichela Ripolone, Dario Ronchi, Raffaella Violano, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS|November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2AFederica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.
Nature Communications|December 21, 2025
Targeted antisense oligonucleotide treatment rescues developmental alterations in spinal muscular atrophy organoidsIrene Faravelli, Paola Rinchetti, Monica Tambalo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 10, 2012
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementiaCinzia Gellera, Cinzia Tiloca, Roberto Del Bo, et al.
Digital Health|March 30, 2026
Minds and machines: AI's transformative role in human identity and medicineStefania Corti, Roberta Ferrucci, Gian Nicola Angotzi, et al.
International Journal of Molecular Sciences|June 2, 2021
Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human PatientsClaudia Malacarne, Mariarita Galbiati, Eleonora Giagnorio, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Pageof 29

Showing results (251-260 of 287) with videos related to

Sort By:
Pageof 29
Cell Death Discovery|March 28, 2026
Lithium ameliorates neural differentiation restoring cell death balance in Cornelia de Lange syndrome 2D and 3D modelsChiara Parodi, Antonella Lettieri, Paolo Grazioli, et al.
JAMA Neurology|April 7, 2015
Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular AtrophyMichela Ripolone, Dario Ronchi, Raffaella Violano, et al.
Journal of Molecular Neuroscience : MN|April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian PatientsDaniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS|November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2AFederica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Journal of Neurology|March 15, 2011
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-upFrancesca Magri, Alessandra Govoni, Maria Grazia D'Angelo, et al.
Nature Communications|December 21, 2025
Targeted antisense oligonucleotide treatment rescues developmental alterations in spinal muscular atrophy organoidsIrene Faravelli, Paola Rinchetti, Monica Tambalo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 10, 2012
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementiaCinzia Gellera, Cinzia Tiloca, Roberto Del Bo, et al.
Digital Health|March 30, 2026
Minds and machines: AI's transformative role in human identity and medicineStefania Corti, Roberta Ferrucci, Gian Nicola Angotzi, et al.
International Journal of Molecular Sciences|June 2, 2021
Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human PatientsClaudia Malacarne, Mariarita Galbiati, Eleonora Giagnorio, et al.
American Journal of Human Genetics|January 29, 2013
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instabilityDario Ronchi, Alessio Di Fonzo, Weiqiang Lin, et al.
Pageof 29